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Catalog Number:
18135
CAS Number:
129295-30-3
6-Fluoro-1H-indazole-3-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
6-Fluoro-3-(1Hindazole carboxylic acid
Documents
$58.39 /250MG
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Product Information

6-Fluoro-1H-indazole-3-carboxylic acid is a versatile compound recognized for its significant role in pharmaceutical research and development. This compound features a unique fluorine atom that enhances its biological activity, making it a valuable building block in the synthesis of various bioactive molecules. Its carboxylic acid functional group contributes to its solubility and reactivity, facilitating its use in diverse chemical reactions. Researchers have utilized 6-Fluoro-1H-indazole-3-carboxylic acid in the development of novel therapeutic agents, particularly in the fields of oncology and neurology, where it has shown promise in targeting specific pathways involved in disease progression.

Additionally, this compound serves as an important intermediate in the synthesis of indazole derivatives, which are known for their anti-inflammatory and analgesic properties. Its unique structural features allow for modifications that can lead to the discovery of new drugs with improved efficacy and reduced side effects. With its growing relevance in medicinal chemistry, 6-Fluoro-1H-indazole-3-carboxylic acid is poised to support advancements in drug discovery and development.

Synonyms
6-Fluoro-3-(1Hindazole carboxylic acid
CAS Number
129295-30-3
Purity
≥ 98% (HPLC)
Molecular Formula
C8H5FN2O2
Molecular Weight
180.14
MDL Number
MFCD03840713
PubChem ID
10821228
Melting Point
? 290 ?C (dec.)
Appearance
White to light beige crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
6-Fluoro-3-(1Hindazole carboxylic acid
CAS Number
129295-30-3
Purity
≥ 98% (HPLC)
Molecular Formula
C8H5FN2O2
Molecular Weight
180.14
MDL Number
MFCD03840713
PubChem ID
10821228
Melting Point
? 290 ?C (dec.)
Appearance
White to light beige crystalline powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Fluoro-1H-indazole-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.
  • Biochemical Research: It is used in studies related to enzyme inhibition and receptor binding, helping researchers understand biological pathways and develop targeted therapies.
  • Material Science: The compound is explored for its potential in creating advanced materials, including polymers and coatings, due to its unique chemical properties.
  • Agricultural Chemistry: It finds applications in the formulation of agrochemicals, contributing to the development of effective herbicides and fungicides to enhance crop protection.
  • Diagnostic Tools: Researchers are investigating its use in the development of diagnostic agents, which can improve the accuracy of medical imaging and disease detection.

Citations